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Reciprocal endoderm-mesoderm interactions mediated byfgf24andfgf10govern pancreas development
Author(s) -
Isabelle Manfroid,
François Delporte,
Ariane Baudhuin,
Patrick Motté,
Carl J. Neumann,
Marianne L. Voz,
Joseph Martial,
Bernard Peers
Publication year - 2007
Publication title -
development
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.754
H-Index - 325
eISSN - 1477-9129
pISSN - 0950-1991
DOI - 10.1242/dev.007823
Subject(s) - mesoderm , endoderm , fgf10 , biology , mesenchyme , fgf and mesoderm formation , intermediate mesoderm , microbiology and biotechnology , zebrafish , pancreas , lateral plate mesoderm , nodal , endocrinology , medicine , fibroblast growth factor , anatomy , embryonic stem cell , embryo , genetics , gene , receptor
In amniotes, the pancreatic mesenchyme plays a crucial role in pancreatic epithelium growth, notably through the secretion of fibroblast growth factors. However, the factors involved in the formation of the pancreatic mesenchyme are still largely unknown. In this study, we characterize, in zebrafish embryos, the pancreatic lateral plate mesoderm, which is located adjacent to the ventral pancreatic bud and is essential for its specification and growth. We firstly show that the endoderm, by expressing the fgf24 gene at early stages, triggers the patterning of the pancreatic lateral plate mesoderm. Based on the expression of isl1, fgf10 and meis genes, this tissue is analogous to the murine pancreatic mesenchyme. Secondly, Fgf10 acts redundantly with Fgf24 in the pancreatic lateral plate mesoderm and they are both required to specify the ventral pancreas. Our results unveil sequential signaling between the endoderm and mesoderm that is critical for the specification and growth of the ventral pancreas, and explain why the zebrafish ventral pancreatic bud generates the whole exocrine tissue.

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